Siemens Axiom Artis zeego systems with software version VC14 — Class II medical device recall Z-0992-2013
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2013-04-03, distributed nationwide. In the course of the firm's product monitoring activities, a potential risk for patient or operators was deter
| Recall number | Z-0992-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2012-11-26 |
| Classified | 2013-03-25 |
| Reported by FDA | 2013-04-03 |
| Terminated | 2013-12-24 |
| Distributed | Nationwide (US) |
| Quantity | 52 |
| Reason classes | software |
| Serial numbers | 160001, 160007, 160008, 160100, 160101, 160122, 160129, 160142, 160149, 160322, 160323, 160347, 160351, 160357, 160373, 160382, 160391, 160395, 160401, 160406, 160411, 160413, 160414, 160421, 160431 and 27 more |
| Model numbers | 10280959 |
Product
Siemens Axiom Artis zeego systems with software version VC14, VC20 and VC21 in conjunction with specific technical configuration Angiographic x-ray system
Reason for recall
In the course of the firm's product monitoring activities, a potential risk for patient or operators was determined during the operation of an Artis zeego system with software revision VC14, VC20 and VC21 in conjunction with a specific technical configuration which cannot be completely executed.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0992-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.